Abstract
Detection and measurement of low-energy beta particles is commonly achieved by liquid scintillation counting, in particular for low-level tritium samples. When samples are contained in plastic scintillation vials for long-term storage, the tritium activity in the vials has been found to decrease faster than expected from its natural radioactive decay. Different explanations for this observation have attributed some of these tritium activity losses to diffusion of the sample, degradation of the LSC cocktail, and the potential long-term changes in quenching effects of the LSC cocktail. An alternative explanation may also be that the tritium organically binds to the carbon chains in the plastic bottle through direct H and H atom exchange. A study was designed and performed to test this latter hypothesis of H and H atom exchange in plastic. Deionized water was introduced in a plastic vial that previously contained tritiated water to assess any increase in tritium activity from the reverse atom exchange between the vial material and the deionized water. A greater loss in activity concentration is observed in plastic vials compared to glass vials as a function of storage time for the tritiated water. Furthermore, the tritium activity concentration in the deionized water increased when storage occurred in plastic vials, an effect that is not observed for storage in glass vials. The study results indicate that hydrogen atom exchange may possibly take place in plastic vials.
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